Gland Pharma's USFDA Nod for Generic Drug

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Jun 04, 2025 16:16

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Gland Pharma receives USFDA approval for Angiotensin II Acetate Injection, gaining 180-day exclusivity. The generic drug treats low blood pressure.
Gland Pharma's USFDA Nod for Generic Drug
New Delhi, Jun 4 (PTI) Gland Pharma on Wednesday said it has received approval from the US health regulator for a generic medication used to increase blood pressure.

The Hyderabad-based firm has received approval from the US Food and Drug Administration (USFDA) for its Abbreviated New Drug Application for Angiotensin II Acetate Injection 2.5 mg/mL, Gland Pharma said in a statement.

Gland Pharma is the exclusive "First-to-File" and is eligible for 180 days of generic drug exclusivity, it stated.


The company's product is therapeutically equivalent to La Jolla Pharma LLC's reference listed drug Giapreza.

The drug is indicated for increasing the blood pressure in adults with septic or other distributive shock.

According to IQVIA, the product had US sales of around USD 58 million for the 12 months ending March 2025.

Gland Pharma shares on Wednesday ended 1.88 per cent up at Rs 1,623.70 apiece on BSE.
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